Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.
This position is part of the Regulatory Affairs Data and Product Release Group within the Medtronic Clinical & Regulatory Solutions (MCRS) organization, supporting regulatory systems and processes. Primary responsibilities include supporting our Unique Device Identification (UDI) process and system to ensure global regulatory compliance and data integrity. Duties may include participating in projects supporting our Regulatory Affairs teams within the Operating Units and Regulatory Operations. This role primarily interfaces with regulatory affairs teams, operating unit (OU) regulatory teams, regulatory operations teams, manager and director.
A role in MCRS offers unique experience opportunities, such as: being part of a global team, collaborating with business partners throughout the company, visibility to global structures and impacts, and insight to various processes and functions across Medtronic.
This role is a hybrid position based in Bogota.
Responsibilities may include the following and other duties may be assigned:
Activities related to enterprise-wide regulatory management systems, including systems coordination, training, developing and implementing plans, and providing input to systems designs.
Performs Regulatory Operations activities including data transformation to support global UDI submissions
Collaborates with global regulatory affairs teams and operation units to gather and analyze required information
Participates actively in cross-functional teams to meet timelines, resolve regulatory issues, and improve work processes.
Required Knowledge and Experience
Bachelor’s degree required
6 months to 1 year of experience
Advanced proficiency in English
High learning agility
Organizational skills and highly detail oriented
Flexible with changing priorities, self-motivated, strong work ethic, works well under pressure in a dynamic environment
Intermediate knowledge of spreadsheet and database applications (Microsoft Office, SharePoint, and Sitebuilder)
Analytical and problem-solving skills
Document interpretation, queries and workflow skills
Excellent communication skills
Nice to Have
Experience in medical device
Experience with regulatory affairs or quality
Experience with UDI
Working knowledge of global regulatory frameworks including MDR (Medical Device Regulation)
Advanced communications skills (written and oral)
Effective project management skills
Physical Job Requirements
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
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Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create.We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).

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